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US5169426A - Cyclohexenone derivatives, their preparation and their use for controlling undesirable plant growth - Google Patents

Cyclohexenone derivatives, their preparation and their use for controlling undesirable plant growth Download PDF

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US5169426A
US5169426A US07/576,197 US57619790A US5169426A US 5169426 A US5169426 A US 5169426A US 57619790 A US57619790 A US 57619790A US 5169426 A US5169426 A US 5169426A
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ethyl
set forth
carbon atoms
epoxy
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Dieter Jahn
Rainer Becker
Michael Keil
Ulrich Schirmer
Bruno Wuerzer
Norbert Meyer
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BASF SE
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BASF SE
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/20—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom three- or four-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02—Compounds containing oxirane rings
    • C07D303/36—Compounds containing oxirane rings with hydrocarbon radicals, substituted by nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D331/00—Heterocyclic compounds containing rings of less than five members, having one sulfur atom as the only ring hetero atom
    • C07D331/02—Three-membered rings

Definitions

  • the present invention relates to cyclohexenone derivatives, herbicides which contain these compounds as active ingredients, and a method for controlling undesirable plant growth.
  • cyclohexenone derivatives can be used for controlling undesirable grasses in broad-leaved crops (DE-A-2 439 104).
  • DE-A-3 219 490 and DE-A-3 032 973 disclose derivatives which are cycloalkenyl-substituted in the 5-position and which likewise possess herbicidal activity.
  • cyclohexenone derivatives of the formula I ##STR2## where A is cycloalkyl radical of 5 to 12 ring members or a bicyclohept-2-yl radical which is fused with an oxirane or thiirane ring, which is unsubstituted or, in the case of cyclohexyl, substituted by not more than three methyl groups, R 1 is hydrogen, methoxycarbonyl or cyano, preferably hydrogen, R 2 is alkyl of 1 to 4 carbon atoms and R 3 is alkyl of 1 to 3 carbon atoms, alkenyl of 3 or 4 carbon atoms, haloalkenyl of 3 or 4 carbon atoms which has 1, 2 or 3 halogen substituents, or propargyl, and salts of these compounds have a good herbicidal action, preferably against species from the grass family (Gramineae). They have a selective action in broad-leaved crops and in monocotyledon crops which do
  • A is a cycloalkyl radical having 5 to 12, preferably 5 to 8, ring members which is fused with an oxirane or thiirane ring which is unsubstituted or, in the case of the cyclohexyl radical, substituted by not more than three methyl groups, e.g.
  • epoxycyclopentyl epoxycyclohexyl, epoxycycloheptyl, epoxycyclooctyl, epoxycyclododecyl, epoxymethylcyclohexyl, dimethylepoxycyclohexyl, epoxytrimethylcyclohexyl, epoxybicycloheptyl, epithiocyclopentyl, epithiocyclohexyl or epithiobicycloheptyl.
  • 3,4-Epoxycyclopentyl is particularly preferred.
  • R 2 is straight-chain or branched alkyl of 1 to 4, preferably 2 or 3, carbon atoms, i.e. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl, isobutyl or tert.-butyl.
  • R 3 is propargyl, alkyl of 1 to 3 carbon atoms, alkenyl of 3 or 4 carbon atoms or haloalkenyl of 3 or 4 carbon atoms which may contain not more than three halogen substituents, e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl, isobutyl, tert.-butyl, allyl, 3-chloroprop-2-enyl, 2-chloroprop-2-enyl, 1,3-dichloroprop-2-enyl or 2,3,3-trichloroprop-2-enyl.
  • halogen substituents e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl, isobutyl, tert.-butyl, allyl, 3-chloroprop-2-enyl, 2-ch
  • Suitable salts of the compounds of the formula I are those which can be used in agriculture, for example the alkali metal salts, in particular the potassium or sodium salts, alkaline earth metal salts, in particular calcium, magnesium or barium salts, manganese, copper, zinc and iron salts, and ammonium, sulfonium and phosphonium salts.
  • the compounds of the formula I can be obtained by reacting a tricarbonyl compound of the formula II ##STR4## where A, R 1 and R 2 have the above meanings, with a hydroxylamine derivative R 3 O--NH 3 Y, where R 3 has the above meaning and Y is an anion.
  • the reaction is advantageously carried out in the heterogeneous phase in an inert diluent at from 0° to 80° C. or from 0° C. to the boiling point of the reaction mixture, in the presence of a base.
  • suitable bases are carbonates, bicarbonates, acetates, alcoholates, hydroxides or oxides of alkali metals or alkaline earth metal, in particular those of sodium, potassium, magnesium and calcium.
  • organic bases such as pyridine or tertiary amines.
  • Suitable diluents are dimethyl sulfoxide, alcohols, such as methanol, ethanol or isopropanol, benzene, hydrocarbons and chlorohydrocarbons, such as chloroform, dichloroethane, hexane or cyclohexane, esters, such as ethyl acetate, and cyclic ethers, such as dioxane or tetrahydrofuran. Mixtures of these diluents may also be used.
  • reaction is complete after a few hours, and the product can then be isolated by evaporating down the mixture, adding water and extracting with a non-polar solvent, such as methylene chloride, and distilling off the solvent under reduced pressure.
  • a non-polar solvent such as methylene chloride
  • the compounds of the formula I may furthermore be obtained by reacting a compound of the formula II with a hydroxylamine of the formula R 3 O--NH 2 , where R 3 has the above meanings, in an inert diluent at from 0° C. to the boiling point of the reaction mixture, in particular from 15° to 70° C. If necessary, the hydroxylamine can be employed in aqueous solution.
  • Suitable diluents for this reaction are alcohols, such as methanol, ethanol, isopropanol or cyclohexanol, hydrocarbons and chlorohydrocarbons, such as hexane, cyclohexane, methylene chloride, toluene or dichloroethane, esters, such as ethyl acetate, nitriles, such as acetonitrile, and cyclic ethers, such as tetrahydrofuran.
  • alcohols such as methanol, ethanol, isopropanol or cyclohexanol
  • hydrocarbons and chlorohydrocarbons such as hexane, cyclohexane, methylene chloride, toluene or dichloroethane
  • esters such as ethyl acetate
  • nitriles such as acetonitrile
  • cyclic ethers such as tetrahydrofur
  • the alkali metal salts of the compounds of the formula I can be obtained by treating these compounds with sodium hydroxide or potassium hydroxide in aqueous solution or in an organic solvent, such as methanol, ethanol or acetone.
  • Sodium alcoholates and potassium alcoholates may also serve as bases.
  • the other metal salts for example the manganese, copper, zinc, iron, calcium, magnesium and barium salts, can be prepared from the sodium salts by reaction with the corresponding metal chlorides in aqueous solution.
  • Ammonium, sulfonium and phosphonium salts can be obtained by reacting compounds of the formula I with ammonium, sulfonium or phosphonium hydroxides, if necessary in aqueous solution.
  • the tricarbonyl compounds of the formula II are novel. They can be prepared by conventional methods (Tetrahedron Lett. 29 (1975), 2491) from cyclohexane-1,3-diones of the formula III, which may also occur in the tautomeric forms IIIa and IIIb ##STR5##
  • the tricarbonyl compounds of the formula II are useful intermediates in the preparation of herbicidal cyclohexenone derivatives of the formula I.
  • Aldehydes of the general formula A'--CHO are well-known or can be obtained in a conventional manner.
  • the oxirane (epoxide) structure can be obtained at the end of the reaction sequence in a conventional manner by reacting the compounds of formula IV with a peroxy compound, such as hydrogen peroxide, tert.-butyl hydroperoxide, performic acid or m-chloroperbenzoic acid, or with atmospheric oxygen.
  • a peroxy compound such as hydrogen peroxide, tert.-butyl hydroperoxide, performic acid or m-chloroperbenzoic acid, or with atmospheric oxygen.
  • the thiirane compounds can be prepared either by reacting the corresponding epoxides with thiocyanates or thiourea, as described in, for example, J. Chem. Soc. 1946, 1050, or by reacting the corresponding unsaturated derivatives with sulfur transfer reagents, such as arylthiosulfenyl chlorides (Chemistry of Heterocyclic Compounds, vol. 42, page 340).
  • the cyclohexanone derivatives of the formula I may be applied for instance in the form of directly sprayable solutions, powders, suspensions (including high-percentage aqueous, oily or other suspensions), dispersions, emulsions, oil dispersions, pastes, dusts, broadcasting agents, or granules by spraying, atomizing, dusting, broadcasting or watering.
  • the forms of application depend entirely on the purpose for which the agents are being used, but they must ensure as fine a distribution of the active ingredient according to the invention as possible.
  • mineral oil fractions of medium to high boiling point such as kerosene or diesel oil, further coal-tar oils, and oils of vegetable or animal origin
  • aliphatic, cyclic and aromatic hydrocarbons such as benzene, toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives such as methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, etc.
  • strongly polar solvents such as dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, water, etc. are suitable.
  • Aqueous formulations may be prepared from emulsion concentrates, pastes, oil dispersions or wettable powders by adding water.
  • emulsions,pastes and oil dispersions the ingredients as such or dissolved in an oil or solvent may be homogenized in water by means of wetting or dispersing agents, adherents or emulsifiers.
  • Concentrates which are suitable for dilution with water may be prepared from active ingredient, wetting agent,adherent, emulsifying or dispersing agent and possibly solvent or oil.
  • surfactants are: alkali metal, alkaline earth metal and ammonium salts of ligninsulfonic acid, naphthalenesulfonic acids, phenolsulfonic acids, alkylaryl sulfonates, alkyl sulfates, and alkyl sulfonates, alkali metal and alkaline earth metal salts of dibutylnaphthalenesulfonic acid, lauryl ether sulfate, fatty alcohol sulfates, alkali metal and alkaline earth metal salts of fatty acids, salts of sulfated hexadecanols, heptadecanols, and octadecanols, salts of sulfated fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensation products of naphthalene or naphthalenesulf
  • Powders, dusts and broadcasting agents may be prepared by mixing or grinding the active ingredients with a solid carrier.
  • Granules e.g., coated, impregnated or homogeneous granules, may be prepared by bonding the active ingredients to solid carriers.
  • solid carriers are mineral earths such as silicic acid, silica gels, silicates, talc, kaolin, attapulgus clay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, and ureas, and vegetable products such as grain flours, bark meal, wood meal, and nutshell meal, cellulosic powders, etc.
  • mineral earths such as silicic acid, silica gels, silicates, talc, kaolin, attapulgus clay, limestone, lime, chalk, bole, loess, clay, dolomite, di
  • the formulations contain from 0.1 to 95, and preferably 0.5 to 90, % by weight of active ingredient.
  • V. 20 parts by weight of compound no. 6 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene-alpha-sulfonic acid, 17parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 60 parts by weight of powdered silica gel, andtriturated in a hammer mill.
  • a spray liquor is obtained containing 0.1% by weight of the active ingredient.
  • the active ingredients may be applied pre- or postemergence. If certain crop plants tolerate the active ingredients lesswell, application techniques may be used in which the herbicidal agents aresprayed from suitable equipment in such a manner that the leaves of sensitive crop plants are if possible not touched, and the agents reach the soil or the unwanted plants growing beneath the crop plants (post-directed, lay-by treatment).
  • the amount of active ingredient applied depends on the time of the year, the plants to be combatted and their growth stage, and varies from 0.025 to 3 kg/ha, but is preferably from 0.05 to 0.5 kg/ha.
  • the vessels employed were plastic flowerpots having a volume of 300 cm 3 , and which were filled with a sandy loam containing about 3.0% humus.
  • the seeds of the test plants were sown shallow, and separately, according to species.
  • the active ingredients were applied to the surface of the soil immediately after the seeds had been sown.
  • the compounds were emulsified or suspended in water as vehicle, and sprayed through finely distributing nozzles.
  • the application rate was 3.0 kg of active ingredient per hectare.
  • the vessels were lightly sprinkler-irrigated to induce germination and growth. Transparent plastic covers were then placedon the vessels until the plants had taken root. The cover ensured uniform germination of the plants, insofar as this was not impaired by the active ingredients.
  • the plants were first grown in the vesselsto a height of from 3 to 15 cm, depending on growth form, before being treated.
  • the soybean plants were grown in a peat-enriched substrate.
  • For this treatment either plants which had been sown directly in the pots andgrown there were selected, or plants which had been grown from seedlings and were transplanted to the pots a few days before treatment.
  • the application rates for postemergence treatment were 0.06 to 0.125 kg of active ingredient per hectare. No covers were placed on the vessels in this method.
  • the pots were set up in the greenhouse--species from warmer areas at from 20° to 35° C., and species from moderate climates at 10° to 25° C. The experiments were run for 2 to 4 weeks. During this period, the plants were tended and their reactions to the various treatments assessed.
  • the scale used for assessment was 0 to 100, 0denoting no damage or normal emergence, and 100 denoting nonemergence or complete destruction of at least the visible plant parts.
  • the plants used in the experiments were Alopecurus myosuroides, Avena fatua, Avena sativa, Digitaria sanguinalis, Echinochloa crus-galli, Glycine max., Lolium multiflorum, Setaria italica, Sinapis alba, Sorghum halepense, Sorghum bicolor, and Zea mays.
  • the compounds used for comparison purposes were 2-(1-allyloxyamino-n-butyl)-5-(cylcohex-1-en-4-yl)-3-hydroxycyclohex-2-en-1-one (A) and 2-(1-ethoximino-n-butyl)-5-(cyclohex-1-en-4-yl)-3-hydroxycyclohex-2-en-1-one (B) disclosed in German DE-A-3 032 973, and 2-(1-ethoxyamino-n-butyl)-5-(cyclooct-1-en-5-yl)-3-hydroxycyclohex-2-en-1-one (C) disclosed in German DE-A-3 219 490, and herbicidal agents containing these compounds.
  • Unwanted grass species were combatted well by, for example, compounds nos. 26, 28, 52, 53, 55 and 61, whereas the broadleaved crop plant alfalfa remained completely undamaged.
  • Compound no. 8 was suitable at low application rates for controlling undesirable grass species, and was tolerated by wheat.
  • the compounds according to may be used in a large number of crop plants.
  • the novel substituted cyclohexenone derivatives may be mixed and applied together with numerous representatives of other herbicidal or growth-regulating active ingredient groups.
  • suitable mixture components are diazines, 4H-3,1-benzoxazine derivatives, benzothiadiazinones, 2,6-dinitroanilines, N-phenylcarbamates, thiolcarbamates, halocarboxylic acids, triazines, amides, ureas, diphenyl ethers, triazinones, uracils, benzofuran derivatives, quinolinecarboxylic acid derivatives, etc.
  • cyclohexenone derivatives of the formulaI may also be useful to apply the cyclohexenone derivatives of the formulaI, either alone or in combination with other herbicides, in admixture with other crop protection agents, e.g., agents for combatting pests or phytopathogenic fungi or bacteria.
  • crop protection agents e.g., agents for combatting pests or phytopathogenic fungi or bacteria.
  • the compounds may also be mixed with solutions of mineral salts used to remedy nutritional or trace element deficiencies. Non-phytotoxic oils and oil concentrates may also be added.

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Abstract

Cyclohexenone derivatives of the formula <IMAGE> where R1, R2, R3 and A have the meanings stated in the description, herbicides which contain these compounds as active ingredients, and a method for controlling undesirable plant growth.

Description

This application is a continuation of Ser. No. 06/935,297, filed Nov. 26, 1986, now abandoned, which is a continuation-in-part of Ser. No. 06/764,324, filed Aug. 12, 1985, now abandoned.
The present invention relates to cyclohexenone derivatives, herbicides which contain these compounds as active ingredients, and a method for controlling undesirable plant growth.
It has been disclosed that cyclohexenone derivatives can be used for controlling undesirable grasses in broad-leaved crops (DE-A-2 439 104). Moreover, DE-A-3 219 490 and DE-A-3 032 973 disclose derivatives which are cycloalkenyl-substituted in the 5-position and which likewise possess herbicidal activity.
We have found that cyclohexenone derivatives of the formula I ##STR2## where A is cycloalkyl radical of 5 to 12 ring members or a bicyclohept-2-yl radical which is fused with an oxirane or thiirane ring, which is unsubstituted or, in the case of cyclohexyl, substituted by not more than three methyl groups, R1 is hydrogen, methoxycarbonyl or cyano, preferably hydrogen, R2 is alkyl of 1 to 4 carbon atoms and R3 is alkyl of 1 to 3 carbon atoms, alkenyl of 3 or 4 carbon atoms, haloalkenyl of 3 or 4 carbon atoms which has 1, 2 or 3 halogen substituents, or propargyl, and salts of these compounds have a good herbicidal action, preferably against species from the grass family (Gramineae). They have a selective action in broad-leaved crops and in monocotyledon crops which do not belong to the Gramineae.
The compounds of the formula I can occur in a plurality of forms, all of which are embraced by the claims: ##STR3##
In formula I, A is a cycloalkyl radical having 5 to 12, preferably 5 to 8, ring members which is fused with an oxirane or thiirane ring which is unsubstituted or, in the case of the cyclohexyl radical, substituted by not more than three methyl groups, e.g. epoxycyclopentyl, epoxycyclohexyl, epoxycycloheptyl, epoxycyclooctyl, epoxycyclododecyl, epoxymethylcyclohexyl, dimethylepoxycyclohexyl, epoxytrimethylcyclohexyl, epoxybicycloheptyl, epithiocyclopentyl, epithiocyclohexyl or epithiobicycloheptyl. 3,4-Epoxycyclopentyl is particularly preferred.
In formula I, R2 is straight-chain or branched alkyl of 1 to 4, preferably 2 or 3, carbon atoms, i.e. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl, isobutyl or tert.-butyl.
In formula I, R3 is propargyl, alkyl of 1 to 3 carbon atoms, alkenyl of 3 or 4 carbon atoms or haloalkenyl of 3 or 4 carbon atoms which may contain not more than three halogen substituents, e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl, isobutyl, tert.-butyl, allyl, 3-chloroprop-2-enyl, 2-chloroprop-2-enyl, 1,3-dichloroprop-2-enyl or 2,3,3-trichloroprop-2-enyl.
Suitable salts of the compounds of the formula I are those which can be used in agriculture, for example the alkali metal salts, in particular the potassium or sodium salts, alkaline earth metal salts, in particular calcium, magnesium or barium salts, manganese, copper, zinc and iron salts, and ammonium, sulfonium and phosphonium salts.
The compounds of the formula I can be obtained by reacting a tricarbonyl compound of the formula II ##STR4## where A, R1 and R2 have the above meanings, with a hydroxylamine derivative R3 O--NH3 Y, where R3 has the above meaning and Y is an anion.
The reaction is advantageously carried out in the heterogeneous phase in an inert diluent at from 0° to 80° C. or from 0° C. to the boiling point of the reaction mixture, in the presence of a base. Examples of suitable bases are carbonates, bicarbonates, acetates, alcoholates, hydroxides or oxides of alkali metals or alkaline earth metal, in particular those of sodium, potassium, magnesium and calcium. It is also possible to use organic bases, such as pyridine or tertiary amines.
Examples of suitable diluents are dimethyl sulfoxide, alcohols, such as methanol, ethanol or isopropanol, benzene, hydrocarbons and chlorohydrocarbons, such as chloroform, dichloroethane, hexane or cyclohexane, esters, such as ethyl acetate, and cyclic ethers, such as dioxane or tetrahydrofuran. Mixtures of these diluents may also be used.
The reaction is complete after a few hours, and the product can then be isolated by evaporating down the mixture, adding water and extracting with a non-polar solvent, such as methylene chloride, and distilling off the solvent under reduced pressure.
The compounds of the formula I may furthermore be obtained by reacting a compound of the formula II with a hydroxylamine of the formula R3 O--NH2, where R3 has the above meanings, in an inert diluent at from 0° C. to the boiling point of the reaction mixture, in particular from 15° to 70° C. If necessary, the hydroxylamine can be employed in aqueous solution.
Examples of suitable diluents for this reaction are alcohols, such as methanol, ethanol, isopropanol or cyclohexanol, hydrocarbons and chlorohydrocarbons, such as hexane, cyclohexane, methylene chloride, toluene or dichloroethane, esters, such as ethyl acetate, nitriles, such as acetonitrile, and cyclic ethers, such as tetrahydrofuran.
The alkali metal salts of the compounds of the formula I can be obtained by treating these compounds with sodium hydroxide or potassium hydroxide in aqueous solution or in an organic solvent, such as methanol, ethanol or acetone. Sodium alcoholates and potassium alcoholates may also serve as bases.
The other metal salts, for example the manganese, copper, zinc, iron, calcium, magnesium and barium salts, can be prepared from the sodium salts by reaction with the corresponding metal chlorides in aqueous solution. Ammonium, sulfonium and phosphonium salts can be obtained by reacting compounds of the formula I with ammonium, sulfonium or phosphonium hydroxides, if necessary in aqueous solution.
The tricarbonyl compounds of the formula II are novel. They can be prepared by conventional methods (Tetrahedron Lett. 29 (1975), 2491) from cyclohexane-1,3-diones of the formula III, which may also occur in the tautomeric forms IIIa and IIIb ##STR5##
It is also possible to prepare the novel compounds of the formula II via the enol-ester intermediates which are obtained, possibly as an isomer mixture, in the reaction of compounds of the formula III, and undergo rearrangement in the presence of an imidazole or pyridine derivative (JP-A-63052/1979).
As is evident from the statements above, the tricarbonyl compounds of the formula II are useful intermediates in the preparation of herbicidal cyclohexenone derivatives of the formula I.
The compounds of the formula III can be obtained by methods which are known from the literature, as is evident from the scheme below: ##STR6##
Aldehydes of the general formula A'--CHO are well-known or can be obtained in a conventional manner.
The oxirane (epoxide) structure can be obtained at the end of the reaction sequence in a conventional manner by reacting the compounds of formula IV with a peroxy compound, such as hydrogen peroxide, tert.-butyl hydroperoxide, performic acid or m-chloroperbenzoic acid, or with atmospheric oxygen.
They can also be synthesized by elimination of hydrogen halide from 1,2-halohydrins generated from the corresponding olefins.
The thiirane compounds can be prepared either by reacting the corresponding epoxides with thiocyanates or thiourea, as described in, for example, J. Chem. Soc. 1946, 1050, or by reacting the corresponding unsaturated derivatives with sulfur transfer reagents, such as arylthiosulfenyl chlorides (Chemistry of Heterocyclic Compounds, vol. 42, page 340).
The Examples which follow illustrate the preparation of the cyclohexenone derivatives of the formula I. Parts by weight bear the same relation to parts by volume as that of the kilogram to the liter.
The 1 H-NMR spectra were recorded on solutions in deuterochloroform as a solvent, using tetramethylsilane as an internal standard. The 1 H chemical shifts are each stated in [ppm]. The following abbreviations were used to describe the signal structure: s=singlet, d=doublet, t=triplet, q=quartet and m=multiplet, strongest signal.
EXAMPLE 1
3.5 parts by weight of 2-butyryl-5-(3,4-epoxycyclohexyl)-cyclohexane-1,3-dione, 1.5 parts by weight of allyloxyammonium chloride and 1.2 parts by weight of sodium bicarbonate in 50 parts by volume of methanol were stirred for 16 hours atroom temperature. The solvent was distilled off under reduced pressure, theresidue was stirred with 50 parts by volume of water and 50 parts by volumeof dichloromethane, the organic phase was separated off, the aqueous phase was extracted once with 50 parts by volume of dichloromethane, the combined organic phases were dried over sodium sulfate and the solvent wasdistilled off under reduced pressure. 2-(1-Allyloxyiminobutyl)-5-(3,4-epoxycyclohexyl)-3-hydroxycyclohex-2-en-1-one (active ingredient No. 1) was obtained.
1 H-NMR spectrum: 0.95 (t), 2.9 (q), 5.3 (m).
EXAMPLE 2
3.5 parts by weight of 2-butyryl-5-(3,4-epoxycyclohexyl)-cyclohexane-1,3-dione and 0.8 part by weight of ethoxyamine in 100 parts by volume of methanol were stirred for 16 hours at room temperature. The solvent was distilled off under reduced pressure, the residue was dissolved in dichloromethane, the solution was washed with 5% strength by weight hydrochloric acid and water and dried over sodium sulfate, and the solvent was distilled off under reduced pressure. 2-(1-Ethoxyiminobutyl)-5-(3,4-epoxycyclohexyl)-3-hydroxycyclohex-2-en-1-one (active ingredient No. 2) was obtained.
1 H-NMR spectrum: 1.3 (t), 3.2 (m), 4.1 (d).
EXAMPLE 3
9 parts by weight of 2-(1-propoxyiminobutyl)-5-(cyclohex-3-enyl)-3-hydroxycyclohex-2-en-1-one were dissolved in 100 parts by weight of dichloromethane, and 5.8 parts byweight of m-chloroperbenzoic acid (about 80%) in 100 parts by volume of dichloromethane were added dropwise at 5°-10° C. After one hour, the course of the reaction was checked by means of thin layer chromatography using a precoated silica gel 60 TLC plate and 1:1 cyclohexane/ethyl acetate as the mobile phase. Further m-chloroperbenzoic acid was added dropwise until conversion was complete. Excess peracid was destroyed by shaking with sodium thiosulfate solution. Thereafter, the mixture was extracted twice with semi-saturated sodium bicarbonate solution and once with water, the organic phase was dried over sodium sulfate and the solvent was distilled off under reduced pressure. 2-(1-Propoxyiminobut-2-yl)-5-(3,4-epoxycyclohexyl)-3-hydroxycyclohex-2-en-1-one (active ingredient No. 3) was obtained.
1 H-NMR spectrum: 2.2 (m), 3.1 (m), 4.0 (q).
The compounds below were obtained by methods similar to those described in the Examples.
__________________________________________________________________________
Active ingre-                                                             
dient no.                                                                 
       A              R.sup.1                                             
                        R.sup.2                                           
                             R.sup.3                                      
                                    .sup.1 H-NMR data                     
__________________________________________________________________________
 4     3,4-epoxy-1-methyl-cyclohexyl                                      
                      H n-propyl                                          
                             ethyl  0.85 (s),1.3 (t),2.9 (m)              
 5     3,4-epoxy-1-methyl-cyclohexyl                                      
                      H n-propyl                                          
                             allyl                                        
 6     3,4-epoxy-4-methyl-cyclohexyl                                      
                      H n-propyl                                          
                             ethyl  1.0 (t),1.3 (s),2.5 (m)               
 7     3,4-epoxy-4-methyl-cyclohexyl                                      
                      H n-propyl                                          
                             allyl                                        
 8     3,4-epoxy-6-methyl-cyclohexyl                                      
                      H n-propyl                                          
                             ethyl  0.95 (t),1.6 (m),4.1 (q)              
 9     3,4-epoxy-6-methyl-cyclohexyl                                      
                      H n-propyl                                          
                             allyl  0.9 (m),2.9 (d),4.55 (d)              
10     3,4-epoxy-6-methyl-cyclohexyl                                      
                      H n-propyl                                          
                             3-chloroallyl                                
                             (trans)                                      
11     1,2-epoxy-2,6,6,-trimethyl-                                        
                      H n-propyl                                          
                             ethyl  1.40 (s),2.9 (m),4.1 (q)              
       cyclohexyl                                                         
12     1,2-epoxy-2,6,6-trimethyl-                                         
                      H n-propyl                                          
                             ethyl                                        
       cyclohexyl                                                         
13     3,4-dimethyl-3,4-epoxy-                                            
                      H n-propyl                                          
                             ethyl  0.95 (t),1.35 (m),4.10 (q)            
       cyclohexyl                                                         
14     3,4-dimethyl-3,4-epoxy-                                            
                      H n-propyl                                          
                             allyl                                        
       cyclohexyl                                                         
15     1,2-epoxy-cyclooctyl                                               
                      H n-propyl                                          
                             ethyl  1.0 (t),1.30 (t),4.1 (q)              
16     1,2-epoxy-cyclooctyl                                               
                      H n-propyl                                          
                             allyl  0.95 (t),1.35 (s),2.95 (m)            
17     4,5-8,9-diepoxy-cyclododecyl                                       
                      H n-propyl                                          
                             ethyl                                        
18     4,5-8,9-diepoxy-cyclododecyl                                       
                      H n-propyl                                          
                             allyl                                        
19     3,4-epoxy-cyclopentyl                                              
                      H n-propyl                                          
                             ethyl                                        
20     3,4-epoxy-cyclopentyl                                              
                      H n-propyl                                          
                             allyl                                        
21     3,4-epoxy-cyclopentyl                                              
                      H n-propyl                                          
                             3-chlorallyl                                 
                             (trans)                                      
22     3,4-epoxy-cyclopentyl                                              
                      H n-propyl                                          
                             propargyl                                    
23     3,4-epoxy-cyclopentyl                                              
                      H ethyl                                             
                             ethyl  1.14 (t),2.9 (q),3.5 (s),4.11 (q)     
24     5,6-epoxy-bicyclo [2.2.1] -                                        
                      H ethyl                                             
                             propargyl                                    
       hept-2-yl                                                          
25     5,6-epoxy-bicyclo [2.2.1]-                                         
                      H ethyl                                             
                             allyl  2.5 (m),2.9 (m),4.55 (d)              
       hept-2-yl                                                          
26     5,6-epoxy-bicyclo [2.2.1]-                                         
                      H ethyl                                             
                             ethyl  0.8 (d)2.5 (m),2.9 (m)                
       hept-2-yl                                                          
27     5,6-epoxy-bicyclo [2.2.1]-                                         
                      H n-propyl                                          
                             3-chloroallyl                                
                                    3.15 (d),4.5 (d),6.3 (m)              
       hept-2-yl             (trans)                                      
28     5,6-epoxy-bicyclo [2.2.1]-                                         
                      H n-propyl                                          
                             ethyl  1.3 (t),2.9 (s),4.1 (q)               
       hept-2-yl                                                          
29     5,6-epoxy-bicyclo [2.2.1]-                                         
                      H n-propyl                                          
                             allyl  1.0 (t),2.5 (m),4.5 (d)               
       hept-2-yl                                                          
30     5,6-epoxy-bicyclo [2.2.1]-                                         
                      H n-propyl                                          
                             propargyl                                    
                                    = 1.0 (t),2.6 (m),4.65 (s)            
       hept-2-yl                                                          
31     2,3-epoxy-cyclohexyl                                               
                      H n-propyl                                          
                             ethyl                                        
32     2,3-epoxy-cyclohexyl                                               
                      H n-propyl                                          
                             allyl                                        
33     3,4-epithio-cyclohexyl                                             
                      H n-propyl                                          
                             ethyl  0.95 (t),2.90 (d),3.15 (m)            
34     3,4-epithio-cyclohexyl                                             
                      H n-propyl                                          
                             allyl                                        
35     5,6-epithio-bicyclo-                                               
                      H n-propyl                                          
                             ethyl                                        
       [2.2.1]hept-2-yl                                                   
36     5,6-epithio-bicyclo-                                               
                      H n-propyl                                          
                             allyl                                        
       [2.2.1]hept-2-yl                                                   
37     3,4-epithio-cyclopentyl                                            
                      H n-propyl                                          
                             ethyl                                        
38     3,4-epithio-cyclopentyl                                            
                      H n-propyl                                          
                             allyl                                        
39     3,4-epithio-cyclopentyl                                            
                      H ethyl                                             
                             allyl                                        
40     3,4-epithio-cyclopentyl                                            
                      H ethyl                                             
                             ethyl                                        
41     2,3-epithio-cyclopentyl                                            
                      H ethyl                                             
                             ethyl                                        
42     2,3-epithio-cyclopentyl                                            
                      H ethyl                                             
                             allyl                                        
43     2,3-epithio-cyclopentyl                                            
                      H n-propyl                                          
                             allyl                                        
44     2,3-epithio-cyclopentyl                                            
                      H n-propyl                                          
                             ethyl                                        
45     2,3-epithio-cyclopentyl                                            
                      H n-propyl                                          
                             3-chloroallyl                                
                             (trans)                                      
46     2,3-epithio-cyclohexyl                                             
                      H n-propyl                                          
                             ethyl                                        
47     2,3-epithio-cyclohexyl                                             
                      H n-propyl                                          
                             allyl                                        
48     2,3-epithio-cyclohexyl                                             
                      H ethyl                                             
                             ethyl                                        
49     2,3-epithio-cyclohexyl                                             
                      H ethyl                                             
                             allyl                                        
50     4,5-epoxy-cyclooctyl                                               
                      H n-propyl                                          
                             ethyl  1.0 (t),1.35 (t),4.1 (q)              
51     4,5-epoxy-cyclooctyl                                               
                      H n-propyl                                          
                             allyl  1.0 (t),2.9 (m),4.55 (d)              
52     4,5-epoxy-cyclooctyl                                               
                      H ethyl                                             
                             ethyl  1.35 (t),2.9 (m),4.1 (q)              
53     4,5-epoxy-cyclooctyl                                               
                      H ethyl                                             
                             allyl  1.15 (t),2.9 (m),4.5 (d)              
54     4,5-epoxy-cyclooctyl                                               
                      H ethyl                                             
                             3-chloroallyl                                
                                    1.15 (t),2.9 (m),4.55 (d)             
                             (trans)                                      
55     4,5-epoxy-cyclooctyl                                               
                      H n-propyl                                          
                             3-chloroallyl                                
                                    0.95 (t),1.5 (m),4.55 (d)             
                             (trans)                                      
56     4,5-8,9-diepoxy-cyclododecyl                                       
                      H ethyl                                             
                             ethyl  1.2 (t),1.3 (m),4.1 (q)               
57     3,4-epoxy-6-methyl-cyclohexyl                                      
                      H ethyl                                             
                             ethyl  1.35 (t),2.9 (q),4.1 (q)              
58     3,4-epoxy-6-methyl-cyclohexyl                                      
                      H ethyl                                             
                             allyl  1.15 (t),2.9 (m),4.5 (d)              
59     2,6-dimethyl-3,4-epoxycyclo-                                       
                      H n-propyl                                          
                             ethyl  1.3 (t),2.9 (s),4.1 (q)               
       hexyl                                                              
60     2,6-dimethyl-3,4-epoxycyclo-                                       
                      H n-propyl                                          
                             3-chloroallyl                                
                                    1.15 (t),28 (m),6.35 (m)              
       hexyl                 (trans)                                      
61     5,6-epoxy-bicyclo[2.2.1]-                                          
                      H ethyl                                             
                             3-chloroallyl                                
                                    1.15 (t),2.5 (m),4.55 (d)             
       hept-2-yl             (trans)                                      
62     3,4-epoxy-cyclohexyl                                               
                      H ethyl                                             
                             ethyl  1.3 (t),3.15 (m),4.1 (q)              
63     3,4-epoxy-cyclohexyl                                               
                      H ethyl                                             
                             allyl  1.15 (t),2.85 (d),4.55 (d)            
64     3,4-epoxy-cyclohexyl                                               
                      H ethyl                                             
                             3-chloroallyl                                
                                    1.1 (t),2.85 (d),6.3 (d)              
                             (trans)                                      
65     3,4-epoxy-2-methylcyclohexyl                                       
                      H n-propyl                                          
                             ethyl  1.6 (q),3.2 (s),4.1 (q)               
66     3,4-epoxy-2-methylcyclohexyl                                       
                      H n-propyl                                          
                             allyl  0.95 (t),1.85 (m),3.20 (s)            
67     3,4-epoxy-2-methylcyclohexyl                                       
                      H ethyl                                             
                             ethyl  1.3 (t),2.35 (m),4.1 (q)              
68     3,4-epoxy-2-methylcyclohexyl                                       
                      H ethyl                                             
                             allyl  2.4 (m),4.6 (d),6.0 (m)               
69     3,4-epoxy-2-methylcyclohexyl                                       
                      H ethyl                                             
                             3-chloroallyl                                
                                    1.15 (t),2.9 (q),4.55 (d)             
                             (trans)                                      
70     3,4-epoxy-cyclopentyl                                              
                      H ethyl                                             
                             allyl  1.13 (t),3.5 (s),4.53 (d),5.36        
                                    (m),5.97 (m)                          
71     3,4-epoxy-cyclopentyl                                              
                      H ethyl                                             
                             3-chloroallyl                                
                                    1.14 (t),3.5 (s),4.55 (d),6.1         
                                    (m),6.35 (d)                          
                             (trans)                                      
72     4,5-epoxy-cycloheptyl                                              
                      H ethyl                                             
                             ethyl                                        
73     4,5-epoxy-cycloheptyl                                              
                      H ethyl                                             
                             allyl                                        
74     4,5-epoxy-cycloheptyl                                              
                      H ethyl                                             
                             3-chloroallyl                                
                             (trans)                                      
75     4,5-epoxy-cycloheptyl                                              
                      H n-propyl                                          
                             3-chloroallyl                                
                             (trans)                                      
76     4,5-epoxy-cycloheptyl                                              
                      H n-propyl                                          
                             ethyl                                        
77     4,5-epoxy-cycloheptyl                                              
                      H n-propyl                                          
                             allyl                                        
__________________________________________________________________________
The cyclohexanone derivatives of the formula I may be applied for instance in the form of directly sprayable solutions, powders, suspensions (including high-percentage aqueous, oily or other suspensions), dispersions, emulsions, oil dispersions, pastes, dusts, broadcasting agents, or granules by spraying, atomizing, dusting, broadcasting or watering. The forms of application depend entirely on the purpose for which the agents are being used, but they must ensure as fine a distribution of the active ingredient according to the invention as possible.
For the preparation of solutions, emulsions, pastes and oil dispersions to be sprayed direct, mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, further coal-tar oils, and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons such as benzene, toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives such as methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, etc., and strongly polar solvents such as dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, water, etc. are suitable.
Aqueous formulations may be prepared from emulsion concentrates, pastes, oil dispersions or wettable powders by adding water. To prepare emulsions,pastes and oil dispersions the ingredients as such or dissolved in an oil or solvent may be homogenized in water by means of wetting or dispersing agents, adherents or emulsifiers. Concentrates which are suitable for dilution with water may be prepared from active ingredient, wetting agent,adherent, emulsifying or dispersing agent and possibly solvent or oil.
Examples of surfactants are: alkali metal, alkaline earth metal and ammonium salts of ligninsulfonic acid, naphthalenesulfonic acids, phenolsulfonic acids, alkylaryl sulfonates, alkyl sulfates, and alkyl sulfonates, alkali metal and alkaline earth metal salts of dibutylnaphthalenesulfonic acid, lauryl ether sulfate, fatty alcohol sulfates, alkali metal and alkaline earth metal salts of fatty acids, salts of sulfated hexadecanols, heptadecanols, and octadecanols, salts of sulfated fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensation products of naphthalene or naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ethers, ethoxylated isooctylphenol, ethoxylated octylphenol and ethoxylated nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ethers, alkylarylpolyether alcohols, isotridecyl alcohol, fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignin, sulfite waste liquors and methyl cellulose.
Powders, dusts and broadcasting agents may be prepared by mixing or grinding the active ingredients with a solid carrier.
Granules, e.g., coated, impregnated or homogeneous granules, may be prepared by bonding the active ingredients to solid carriers. Examples of solid carriers are mineral earths such as silicic acid, silica gels, silicates, talc, kaolin, attapulgus clay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, and ureas, and vegetable products such as grain flours, bark meal, wood meal, and nutshell meal, cellulosic powders, etc.
The formulations contain from 0.1 to 95, and preferably 0.5 to 90, % by weight of active ingredient.
Examples of formulations are given below.
I. 90 parts by weight of compound no. 1 is mixed with 10 parts by weight ofN-methyl-alpha-pyrrolidone. A mixture is obtained which is suitable for application in the form of very fine drops.
II. 20 parts by weight of compound no. 2 is dissolved in a mixture consisting of 80 parts by weight of xylene, 10 parts by weight of the adduct of 8 to 10 moles of ethylene oxide and 1 mole of oleic acid-N-monoethanolamide, 5 parts by weight of the calcium salt of dodecylbenzenesulfonic acid, and 5 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and uniformly distributing it therein, an aqueous dispersion is obtained containing 0.02% by weight of the active ingredient.
III. 20 parts by weight of compound no. 1 is dissolved in a mixture consisting of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the adduct of 7 moles of ethylene oxide and 1 mole of isooctylphenol, and 10 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and finely distributing it therein, an aqueous dispersion is obtained containing 0.02% by weight of the activeingredient.
IV. 20 parts by weight of compound no. 4 is dissolved in a mixture consisting of 25 parts by weight of cyclohexanol, 65 parts by weight of a mineral oil fraction having a boiling point between 210° and 280° C., and 10 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and uniformly distributing it therein, anaqueous dispersion is obtained containing 0.02% by weight of the active ingredient.
V. 20 parts by weight of compound no. 6 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene-alpha-sulfonic acid, 17parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 60 parts by weight of powdered silica gel, andtriturated in a hammer mill. By uniformly distributing the mixture in 20,000 parts by weight of water, a spray liquor is obtained containing 0.1% by weight of the active ingredient.
VI. 3 parts by weight of compound no. 13 is intimately mixed with 97 parts by weight of particulate kaolin. A dust is obtained containing 3% by weight of the active ingredient.
VII. 30 parts by weight of compound no. 11 is intimately mixed with a mixture consisting of 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil which has been sprayed onto the surface ofthis silica gel. A formulation of the active ingredient is obtained having good adherence.
VIII. 20 parts of compound no. 1 is intimately mixed with 2 parts of the calcium salt of dodecylbenzenesulfonic acid, 8 parts of a fatty alcohol polyglycol ether, 2 parts of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate and 68 parts of a paraffinic mineral oil. A stable oily dispersion is obtained.
The active ingredients, or agents containing them, may be applied pre- or postemergence. If certain crop plants tolerate the active ingredients lesswell, application techniques may be used in which the herbicidal agents aresprayed from suitable equipment in such a manner that the leaves of sensitive crop plants are if possible not touched, and the agents reach the soil or the unwanted plants growing beneath the crop plants (post-directed, lay-by treatment).
The amount of active ingredient applied depends on the time of the year, the plants to be combatted and their growth stage, and varies from 0.025 to 3 kg/ha, but is preferably from 0.05 to 0.5 kg/ha.
The action of the cyclohexenone derivatives of the formula I on plant growth is demonstrated in greenhouse experiments.
The vessels employed were plastic flowerpots having a volume of 300 cm3, and which were filled with a sandy loam containing about 3.0% humus. The seeds of the test plants were sown shallow, and separately, according to species. For the preemergence treatment, the active ingredients were applied to the surface of the soil immediately after the seeds had been sown. The compounds were emulsified or suspended in water as vehicle, and sprayed through finely distributing nozzles. The application rate was 3.0 kg of active ingredient per hectare. After the agents had been applied, the vessels were lightly sprinkler-irrigated to induce germination and growth. Transparent plastic covers were then placedon the vessels until the plants had taken root. The cover ensured uniform germination of the plants, insofar as this was not impaired by the active ingredients.
For the postemergence treatment, the plants were first grown in the vesselsto a height of from 3 to 15 cm, depending on growth form, before being treated. The soybean plants were grown in a peat-enriched substrate. For this treatment, either plants which had been sown directly in the pots andgrown there were selected, or plants which had been grown from seedlings and were transplanted to the pots a few days before treatment. The application rates for postemergence treatment were 0.06 to 0.125 kg of active ingredient per hectare. No covers were placed on the vessels in this method.
The pots were set up in the greenhouse--species from warmer areas at from 20° to 35° C., and species from moderate climates at 10° to 25° C. The experiments were run for 2 to 4 weeks. During this period, the plants were tended and their reactions to the various treatments assessed. The scale used for assessment was 0 to 100, 0denoting no damage or normal emergence, and 100 denoting nonemergence or complete destruction of at least the visible plant parts.
The plants used in the experiments were Alopecurus myosuroides, Avena fatua, Avena sativa, Digitaria sanguinalis, Echinochloa crus-galli, Glycine max., Lolium multiflorum, Setaria italica, Sinapis alba, Sorghum halepense, Sorghum bicolor, and Zea mays.
The compounds used for comparison purposes were 2-(1-allyloxyamino-n-butyl)-5-(cylcohex-1-en-4-yl)-3-hydroxycyclohex-2-en-1-one (A) and 2-(1-ethoximino-n-butyl)-5-(cyclohex-1-en-4-yl)-3-hydroxycyclohex-2-en-1-one (B) disclosed in German DE-A-3 032 973, and 2-(1-ethoxyamino-n-butyl)-5-(cyclooct-1-en-5-yl)-3-hydroxycyclohex-2-en-1-one (C) disclosed in German DE-A-3 219 490, and herbicidal agents containing these compounds.
On preemergence application, compounds nos. 4, 6, 11 and 13, for instance, had a herbicidal action on plants from the grasses family, whereas Sinapisalba, as a dicotyledonous representative, remained completely undamaged.
For example compounds nos. 4 and 6, applied postemergence at a rate of 0.125 kg/ha, had a strong herbicidal action on a broad spectrum of grassy weeds; soybeans, as dicotyledonous crop plants, suffered no damage whatsoever.
Unwanted grass species were combatted well by, for example, compounds nos. 26, 28, 52, 53, 55 and 61, whereas the broadleaved crop plant alfalfa remained completely undamaged.
Compound no. 8, for example, was suitable at low application rates for controlling undesirable grass species, and was tolerated by wheat.
Compounds nos. 1 and 2 selected by way of example control problem grasses much better than prior art comparative agents A and B, and are fully tolerated by soybeans.
Compared with prior art agent C, the degree of herbicidal action of, for instance, compound no. 50 is significantly higher, without compatibility for alfalfa being influenced.
In view of the spectrum of weeds which can be combatted, the tolerance of the active ingredients according to the invention by crop plants, the desired influence on the growth of crop plants, and in view of the numerous application methods possible, the compounds according to may be used in a large number of crop plants.
The following may be mentioned by way of example:
______________________________________                                    
Botanical name     Common name                                            
______________________________________                                    
Allium cepa        onions                                                 
Ananas comosus     pineapples                                             
Arachis hypogaea   peanuts (groundnuts)                                   
Aaparagus officinalis                                                     
                   asparagus                                              
Avena sativa       oats                                                   
Beta Vulgaris spp. altissima                                              
                   sugarbeets                                             
Beta vulgaris spp. rapa                                                   
                   fodder beets                                           
Beta vulgaris spp. esculenta                                              
                   table beets, red beets                                 
Brassica napus var. napus                                                 
                   rapeseed                                               
Brassica napus var. napobrassica                                          
                   swedes                                                 
Brassica napus var. rapa                                                  
                   turnips                                                
Brassica rapa var. silvestris                                             
Camellia sinensis  tea plants                                             
Carthamus tinctorius                                                      
                   safflower                                              
Carya illinoinensis                                                       
                   pecan trees                                            
Citrus limon       lemons                                                 
Citrus maxima      grapefruits                                            
Citrus reticulata  mandarins                                              
Citrus sinensis    orange trees                                           
Coffea arabica (Coffea canephora,                                         
                   coffee plants                                          
Coffea liberica)                                                          
Cucumis melo       melons                                                 
Cucumis sativus    cucumbers                                              
Cynodon dactylon   Bermudagrass in turf                                   
                   and lawns                                              
Daucus carota      carrots                                                
Elais guineensis   oil palms                                              
Fragaria vesca     strawberries                                           
Glycine max        soybeans                                               
Gossypium hirsutum cotton                                                 
(Gossypium arboreum                                                       
Gossypium herbaceum                                                       
Gossypium vitifolium)                                                     
Helianthus annuus  sunflowers                                             
Helianthus tuberosus                                                      
                   Jerusalem artichoke                                    
Hevea brasiliensis rubber plants                                          
Hordeum vulgare    barley                                                 
Humulus lupulus    hops                                                   
 Ipomoea batatas   sweet potatoes                                         
Juglans regia      walnut trees                                           
Lactuca sativa     lettuce                                                
Lens culinaris     lentils                                                
Linum usitatissimum                                                       
                   flax                                                   
Lycopersicon lycopersicum                                                 
                   tomatoes                                               
Malus spp.         apple trees                                            
Manihot esculenta  cassava                                                
Medicago sativa    alfalfa (lucerne)                                      
Mentha piperita    peppermint                                             
Musa spp.          banana plants                                          
Nicothiana tabacum tobacco                                                
(N. rustica)                                                              
Olea europaea      olive trees                                            
Oryza sativa       rice                                                   
Panicum miliaceum  millet                                                 
Phaseolus lunatus  limabeans                                              
Phaseolus mungo    mungbeans                                              
Phaseolus vulgaris snapbeans, green beans,                                
                   dry beans                                              
Pennisetum glaucum pearl millet                                           
Petroselinum crispum                                                      
                   parsley                                                
spp. tuberosum                                                            
Picea abies        Norway spruce                                          
Abies alba         fir trees                                              
Pinus spp.         pine trees                                             
Pisum sativum      English peas                                           
Prunus avium       cherry trees                                           
Prunus domestica   plum trees                                             
Prunus dulcis      almond trees                                           
Prunus persica     peach trees                                            
Pyrus communis     pear trees                                             
Ribes sylvestre    redcurrants                                            
Ribes uva-crispa   gooseberries                                           
Ricinus communis   castor-oil plants                                      
Saccharum officinarum                                                     
                   sugar cane                                             
Secale cereale     rye                                                    
Sesamum indicum    sesame                                                 
Solanum tuberosum  Irish potatoes                                         
Sorghum bicolor (s. vulgare)                                              
                   sorghum                                                
Sorghum dochna     sorgo                                                  
Spinacia oleracea  spinach                                                
Theobroma cacao    cacao plants                                           
Trifolium pratense red clover                                             
Triticum aestivum  wheat                                                  
Vaccinium corymbosum                                                      
                   blueberries                                            
Vaccinium vitis-idaea                                                     
                   cranberries                                            
Vicia faba         tick beans                                             
Vigna sinnensis (V. unguiculata)                                          
                   cow peas                                               
Vitis vinifera     grapes                                                 
Zea mays           Indian corn, sweet                                     
                   corn, maize                                            
                   (post-directed)                                        
______________________________________
To increase the spectrum of action and to achieve synergistic effects, the novel substituted cyclohexenone derivatives may be mixed and applied together with numerous representatives of other herbicidal or growth-regulating active ingredient groups. Examples of suitable mixture components are diazines, 4H-3,1-benzoxazine derivatives, benzothiadiazinones, 2,6-dinitroanilines, N-phenylcarbamates, thiolcarbamates, halocarboxylic acids, triazines, amides, ureas, diphenyl ethers, triazinones, uracils, benzofuran derivatives, quinolinecarboxylic acid derivatives, etc.
It may also be useful to apply the cyclohexenone derivatives of the formulaI, either alone or in combination with other herbicides, in admixture with other crop protection agents, e.g., agents for combatting pests or phytopathogenic fungi or bacteria. The compounds may also be mixed with solutions of mineral salts used to remedy nutritional or trace element deficiencies. Non-phytotoxic oils and oil concentrates may also be added.

Claims (9)

We claim:
1. A cyclohexenone derivative of the formula ##STR7## where A is an unsubstituted monocyclic cycloalkyl radical of 5 to 12 ring members or a cyclohexyl radical substituted by one to three methyl groups, wherein both said cycloalkyl and cyclohexyl radicals have two adjacent ring carbon atoms bridged by an oxygen or sulfur atom to form a fused oxirane or thiirane ring, or A is a 5,6-epoxybicylohept-2-yl radical, R1 is hydrogen, methoxycarbonyl or cyano, R2 is alkyl of 1 to 4 carbon atoms and R3 is alkyl of 1 to 3 carbon atoms, alkenyl of 3 or 4 carbon atoms, haloalkenyl of 3 or 4 carbon atoms which has 1, 2 or 3 halogen substituents, or propargyl, or a salt thereof.
2. A cyclohexenone derivative of the formula I as set forth in claim 1, wherein R1 is hydrogen.
3. A cyclohexenone derivative of the formula I as set forth in claim 1, where A is an unsubstituted monocyclic cycloalkyl radical of from 5 to 8 ring members or a cyclohexyl radical substituted by one to three methyl groups, wherein both said cycloalkyl and cyclohexyl radicals have two adjacent ring carbon atoms bridged by an oxygen or sulfur atom to form a fused oxirane or thiirane ring, or A is a 5,6-epoxybicyclo-hept-2-yl radical.
4. A cyclohexenone derivative of the formula I as set forth in claim 1, where A is 3,4-epoxycyclopentyl.
5. A cyclohexenone derivative of the formula I as set forth in claim 1, where R2 is alkyl of 2 or 3 carbon atoms.
6. A herbicidal composition containing inert additives and a herbicidally effective amount of a cyclohexenone derivative of the formula I as set forth in claim 1.
7. A herbicidal composition as set forth in claim 6, containing from 0.1 to 95 wt % of a cyclohexenone derivative of the formula I.
8. A herbicidal composition as set forth in claim 6, where R1 in the cyclohexenone derivative of the formula I is hydrogen.
9. A process for combatting the growth of unwanted plants, wherein the unwanted plants or the areas to be kept free from unwanted plant growth are treated with a herbicidally effective amount of a cyclohexenone derivative of the formula I as set forth in claim 1.
US07/576,197 1984-08-18 1990-08-30 Cyclohexenone derivatives, their preparation and their use for controlling undesirable plant growth Expired - Fee Related US5169426A (en)

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DE3430483 1984-08-18
DE3430483 1984-08-18
DE19853502391 DE3502391A1 (en) 1984-08-18 1985-01-25 CYCLOHEXENON DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH
DE3502391 1985-01-25
US76432485A 1985-08-12 1985-08-12
US93529786A 1986-11-26 1986-11-26
US07/576,197 US5169426A (en) 1984-08-18 1990-08-30 Cyclohexenone derivatives, their preparation and their use for controlling undesirable plant growth

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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3773824A (en) * 1971-06-14 1973-11-20 Mobil Oil Corp 3-(4-methyl-3-cyclohexenyl)butyl esters of organic acids

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3773824A (en) * 1971-06-14 1973-11-20 Mobil Oil Corp 3-(4-methyl-3-cyclohexenyl)butyl esters of organic acids

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